Decreased functional concordance in male children with autism spectrum disorder

Author:

Lu Huibin12,Wang Sha12,Xue Zaifa12,Liu Jing12,Niu Xiaoxia12,Gao Le12,Guo Xiaonan12ORCID

Affiliation:

1. School of Information Science and Engineering Yanshan University Qinhuangdao China

2. Hebei Key Laboratory of Information Transmission and Signal Processing Yanshan University Qinhuangdao China

Abstract

AbstractAutism spectrum disorder (ASD) is an early‐onset neurodevelopmental condition with altered function of the brain. At present, a variety of functional metrics from neuroimaging techniques have been used to explore ASD neurological mechanisms. However, the concordance of these functional metrics in ASD is still unclear. This study used resting‐state functional magnetic resonance imaging data, which were obtained from the open‐access Autism Brain Imaging Data Exchange database, including 105 children with ASD and 102 demographically matched typically developing (TD) children. Both voxel‐wise and volume‐wise functional concordance were calculated by combining the dynamic amplitude of low‐frequency fluctuations, dynamic regional homogeneity, and dynamic global signal correlation. Furthermore, a two‐sample t‐test was performed to compare the functional concordance between ASD and TD groups. Finally, the relationship between voxel‐wise functional concordance and Autism Diagnostic Observation Schedule subscores was analyzed using the multivariate support vector regression in the ASD group. Compared with the TD group, we found that ASD showed decreased voxel‐wise functional concordance in the left superior temporal pole (STGp), right amygdala, and left opercular part of the inferior frontal gyrus (IFGoper). Moreover, decreased functional concordance was associated with restricted and repetitive behaviors in ASD. Our results found altered brain function in the left STGp, right amygdala, and left IFGoper in ASD by functional concordance, indicating that functional concordance may provide new insights into the neurological mechanisms of ASD.

Funder

Natural Science Foundation of Hebei Province

National Natural Science Foundation of China

Publisher

Wiley

Subject

Genetics (clinical),Neurology (clinical),General Neuroscience

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